Microanchors for anchoring devices to body tissues

ABSTRACT

Tissue anchoring devices in the form of microanchors that partially penetrate tissue, thereby avoiding full thickness penetration of the tissue, yet are secure enough to enable reliable device fixation and easy removal of the device.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 16/271,253, filed Feb. 8, 2019, which is a continuation of U.S. application Ser. No. 13/961,367, filed Aug. 7, 2013, now U.S. Pat. No. 10,226,270, issued Mar. 12, 2019, which claims priority to U.S. Provisional Application No. 61/681,673, filed Aug. 10, 2012, all of which are incorporated herein by reference in their entireties for all purposes.

FIELD OF THE INVENTION

The present invention is directed to microanchors for anchoring devices to body tissues, and more particularly, to microanchoring devices that enable reliable device fixation and easy removal of the device.

BACKGROUND OF THE INVENTION

Implantable devices such as intestinal sleeves are known in the industry. A common difficulty associated with such devices that are designed for implantation in the GI tract is reliable anchoring of the devices. The GI tract is a very dynamic area of the body. There is much movement, flow, and other disruptive action that exerts forces on the implanted device. Anchoring the device so that it stays in place without migration in these dynamic locations is very difficult. The tissue anchors must be secure enough to anchor endolumenally delivered devices in the GI tract and yet produce minimal impact to normal physiological functions of the GI tract, such as motility, blood supply to the surrounding tissue, secretions, patency, etc.). In addition, the tissue anchors must avoid causing pain to the patient.

An even greater challenge is presented with temporary implantable devices—those that are designed to be anchored in the body fora limited period of time, and then removed. The tissue anchors for these devices must meet all of the same criteria for reliable fixation and allowing normal GI tract functions, but must also permit endolumenal removal of the device. A tissue anchor satisfying all of these needs is highly desirable.

SUMMARY OF THE INVENTION

The present invention provides tissue anchors in the form of microanchors, the length of which ensure penetration of only the submucosa of the tissue, yet are secure enough to enable reliable device fixation and easy removal of the device while maintaining normal GI tract functions. The invention includes several embodiments of these m icroanchors.

In a first embodiment, the present invention provides a microanchor comprising a first tissue engagement member, a second tissue engagement member, and a strain relieving connector joining the first tissue engagement member to the second tissue engagement member, wherein said device has a retracted state and an engaged state, the first tissue engagement member and said second tissue engagement member forming a pincer in the engaged state.

In another embodiment, the present invention provides a microanchor for fixating a device within a body lumen comprising a first portion attached to said device, a second portion having at least one tissue engagement member for insertion into a wall of the body lumen, and a reversibly deformable and recoverable segment located between the first portion and the second portion.

In a third embodiment, the present invention provides a microanchor comprising a central hub and at least three tissue engagement members radially oriented on the central hub, wherein the device has a constrained state and an engaged state, and wherein the tissue engagement members are in apposition to each other in the engaged state.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A is a perspective view of an exemplary embodiment of the invention in a retracted state.

FIG. 1B is a perspective view of the microanchor of FIG. 1A in an engaged state. FIG. 1C is a perspective view of microanchors of FIG. 1A mounted on a stent graft attached to a graft.

FIG. 1D is a perspective view of microanchors of FIG. 1A mounted on a sleeve.

FIG. 2A is a perspective view of another exemplary embodiment of the present invention.

FIG. 2B is a perspective view of microanchors of FIG. 2A mounted on a sleeve

FIG. 3A is a perspective view of another exemplary embodiment of the present invention in a retracted state.

FIG. 3B is a perspective view of the microanchor of FIG. 3A in an engaged state.

FIG. 3C is a perspective view of microanchors of FIG. 3A coupled to an implantable device.

FIG. 3D is a perspective view of microanchors of FIG. 3A coupled to an implanted device in an engaged state.

FIG. 4A is a perspective view of another exemplary embodiment of the present invention

FIG. 4B is a perspective view of microanchors of FIG. 4A coupled to an end portion of an implantable sleeve device. FIG. 4C is a perspective view of microanchors of FIG. 4A coupled to an end region of an implantable sleeve device.

FIG. 4D is a perspective view of microanchors of FIG. 4A coupled to an implantable device comprising a stent portion and a graft portion.

FIG. 5 is a perspective view of another exemplary embodiment of the present invention

DETAILED DESCRIPTION OF THE INVENTION

The present invention will now be described with reference to exemplary embodiments. In a first embodiment illustrated in FIGS. 1A and 1B, a microanchor device 1 is illustrated having a first tissue engagement member 10 and second tissue engagement member 11 joined by a connector 12. Connector 12 in this embodiment is a coil spring made of a metal such as nitinol or stainless steel. Other biocompatible materials may also be used provided that they can be repeatedly retracted and engaged as described herein including but not limited to chrome cobalt alloys such as Elgiloy or L605 and titanium alloys such as Titanium Beta 3. FIG. 1A illustrates the microanchor device 1 in a retracted state. In this retracted state, first tissue engagement member 10 and second tissue engagement member 11 are physically wound against the tension of the spring such that they are in proximity to each other. The engagement members 10 and 11 are then physically constrained using external means such as a suture or ligament or line 15. Line 15 is tied around both engagement members 10 and 11 to physically constrain them in retracted state. The force of the spring coil connector 12 is stored as potential energy in this retracted state. It should be understood that the use of tethers to restrain tissue engagement members is merely exemplary and that any thermal or mechanical means to initially restrain tissue engagement members could be employed. In one embodiment, a rigid sheath could be employed to restrain tissue engagement members.

In use, a plurality of microanchor devices 1 as illustrated in FIG. 1A are mounted around a portion of a device to be anchored within the body. For example, as illustrated in FIG. 1C, microanchor devices 1 are mounted at various locations on a stent frame 19 of a device to be anchored within a body. As illustrated in FIG. 1C, microanchor devices 1 are mounted at the apices of the stent frame and are depicted in their restrained state. The stent frame is optionally used in combination with a graft member 16 which may extend any desired length, including beyond the stent frame 19.

For insertion into a body, the stent frame 19 and any associated graft 16 are diametrically compressed into a small configuration suitable for insertion into a catheter device, for example. The stent frame 19 and any associated graft 16 are then advanced along the catheter to the desired point of deployment within the body. At that point, the stent frame 19 and any associated graft 16 are deployed from the catheter and expand to the desired diametrical size to engage the tissue or vessel walls.

After deployment of stent, the operator, typically a doctor, will manipulate tether lines 15 (as shown in FIG. 1A), which will in turn release first tissue engagement member 10, and second tissue engagement member 11. At that point, as illustrated in FIG. 1B, microanchor device 1 releases the stored potential energy within connector 12 and forces first tissue engagement member 10 and second tissue engagement member 11 into an engaged state, illustrated in FIG. 1B. In this engaged state, first tissue engagement member 10 and second tissue engagement member 11 form a pincer. By “pincer” as used herein is meant a configuration in which first tissue engagement member 10 and second tissue engagement member 11 are essentially two grasping jaws working on a pivot used for gripping tissue 18.

With reference again to FIG. 1C, once all of the microanchor devices 1 have been deployed from their retracted state to their engaged state, the stent frame 19 and any associated graft 16 are anchored securely to the body tissue. Although this anchoring is secured, it is not necessarily permanent. Microanchor device 1 is designed to penetrate only the sub-mucosa of the tissue. The microanchors described herein, typically penetrate less than one millimeter into the tissue. As a result, with the application of appropriate force in the appropriate direction, microanchor device 1 can be disengaged or removed from the tissue 18. In this way, the stent frame 19 and any associated graft 16 can be removed from the body after disengaging microanchor devices 1.

An alternate device configuration is illustrated in FIG. 1D where a plurality of microanchor devices 1 as illustrated in FIG. 1A are mounted at various locations of a sleeve device 16 to be anchored within a body without the use of a stent. As illustrated in FIG. 1D, microanchor devices 1 are mounted directly on graft member 16 and are depicted in their restrained state. The anchoring devices 1 may mounted on a portion of the graft, such as the proximal length of the graft, or may mounted throughout the length of the graft (figure not shown). The microanchors could be attached individually to the sleeve and oriented in parallel to resist distal movement of the sleeve. Alternatively, the anchors could be randomly oriented. In another embodiment, the microanchors could be attached to one another to form a chain which is subsequently attached to the sleeve.

The device shown in FIG. 1D may be packed into a small configuration suitable for insertion into a catheter device. For deployment the packed device may be advanced along the catheter to the desired point of deployment within the body. After deployment the tissue engagement members on graft 16 may be put in the proximity of the tissue, through a tissue approximation mechanism. An example of the tissue approximation mechanism is use of an inflating balloon to put graft 16 and the microanchor device 1 in proximity of the tissue that it will engage.

After approximating the microanchor device 1 to the tissue, the operator, typically a doctor, will manipulate tether lines 15, which will in turn release first tissue engagement member 10, and second tissue engagement member 11, by releasing (as illustrated in FIG. 1B) the stored potential energy within connector 12 and forming the pincer as described earlier to engage the tissue.

A second embodiment of the present invention is illustrated in FIG. 2A. In FIG. 2A, a microanchor device 2 is shown. The microanchor device 2 has a first portion 20, a second portion 21, and a connector portion 23 connecting the first portion 20 to the second portion 21. The first portion 20 is adapted for attachment to an apparatus to be anchored within the body. The second portion 21 of the microanchor device 2 has a tissue engagement member 22 adapted for insertion into body tissue. The tissue engagement member 22 may be a microanchor that is dimensioned to only extend into the submucosa of the tissue upon implantation and deployment of the microanchor device 2. The size of the tissue engagement member 22 is limited so that the anchoring member 22 does not extend through the wall of the tissue and so that upon removal the tissue engagement member does not tear the tissue.

The first portion 20 and second portion 21 of the microanchor device 2 are coupled together through a reversibly deformable or resilient connector portion 23. Upon implantation of the apparatus in a body, the tissue engagement member 22 is engaged with a body tissue and the first portion 20 is coupled to the apparatus. As the body exerts forces on the implanted apparatus, the apparatus may move in response to these external forces. The resilient or reversibly deformable portion 23 may provide a strain relief that may absorb these forces by stretching or deforming along the length of the deformable portion 23. The dissipation of the force should reduce the likelihood of the engagement member 22 disengaging from the tissue. The application of a force to the apparatus will cause connector segment 23 to stretch or deform, thus absorbing the shock or energy from the force without directly exerting that force through the tissue engagement member on the tissue itself.

In the embodiment illustrated in FIG. 2A, connector segment 23 is formed of the same wire as the rest of the microanchor device, which can be a material such as nitinol or stainless steel or other reversibly deformable (resilient) material. Connector segment 23 in the illustrated embodiment is shaped in the form of an “S”. Upon application of a force to first portion 20, the “S” connector segment 23 straightens out or substantially straightens out (stretches or lengthens) to absorb the shock. The deformation of the “S” shape may reduce the amount of force that will transfer through the first portion 20 of the microanchor device 2 to the second portion 21 and the engagement member 22. The connector segment 23 absorbs the force in order to reduce the likelihood of tissue engagement member 22 pulling out of the tissue. Upon release of the force, connector segment 23 then reversibly regains its initial “S” shape, ready to deform again to absorb further forces on microanchor device 2. In this way, when a plurality of microanchor devices 2 of this embodiment are disposed around an apparatus anchored within a body, the microanchor devices 2 are able to absorb the repeated shock of forces applied to the device, such as within the intestine. The apparatus anchored within the intestine is thereby securely maintained.

As with the microanchor device illustrated in FIGS. 1A-1C, the tissue engagement member 22 of microanchor device 2 only penetrates the submucosa of the tissue. Therefore upon application of an appropriate force to tissue engagement member 22, it may be removed from the tissue, thereby allowing the apparatus to be removed from the body with minimal injury or tearing to the tissue wall.

In use, a plurality of microanchor devices as illustrated in FIG. 2A can be mounted around a portion of a device to be anchored within the body. For example, as illustrated in FIG. 2B, a plurality of microanchor devices 2 are mounted at various locations of a sleeve device 16 to be anchored within a body without the use of a stent. The microanchors could be attached individually to the sleeve and oriented in parallel to resist distal movement of the sleeve. Alternatively, the anchors could be randomly oriented.

The device shown in FIG. 2B may be packed into a small configuration suitable for insertion into a catheter device. For deployment the packed device may be advanced along the catheter to the desired point of deployment within the body. After deployment, the tissue engagement members of microanchor devices 2 on graft 16 may be put in the proximity of the tissue, through a tissue approximation mechanism. An example of the tissue approximation mechanism is use of an inflating balloon to put graft 16 and the microanchor device 2 in proximity of the tissue that it will engage.

After approximating the microanchor device 2 to the tissue, the operator, typically a doctor, will manipulate the engagement members with the tissue by pulling on the catheter, which would set the engagement members into the tissue.

Another embodiment of the present invention is illustrated in FIGS. 3A-3D. As shown in FIG. 3A, a microanchor device 3 has a central hub 30 and a plurality of tissue engagement members 31 extending therefrom. Typically this microanchor device 3 is formed of a shape memory material such as nitinol. The configuration illustrated in FIG. 3A depicts the device in a retracted state. A plurality of microanchor devices 3 may be mounted around an apparatus to be anchored within a body, such as around a stent frame of such device, as shown in FIGS. 3C & 3D. Upon insertion and deployment of the apparatus at the desired location within the body, microanchor device 3 is released from its retracted state into an engaged state, as illustrated in FIG. 3B. Typically, with shape memory metals, this release from retracted state to engaged state is stress induced, however, it is envisioned that this activation could be thermally induced as well. In an engaged state, tissue engagement members 31 are in apposition to each other. This means that they are facing substantially toward one another in a configuration that effectively grips the body tissue. As with the previous two embodiments, microanchor device 3 is adapted to only penetrate the submucosa, approximately one millimeter, in the tissue. As a result, upon application of suitable force, it can be removed from the tissue. Nonetheless, the apparatus anchored by the microanchor device 3 is securely maintained at its position within the body, enduring the forces and shock experienced by the apparatus, holding it securely in place. The multiple directions of the anchor members allow the device to withstand the forces that are within a body lumen. These forces may not be in a single direction and the multiple directions of the anchor members allow the device to be maintained within the lumen.

Turning now to FIGS. 3C and 3D, the m icroanchor device 3 is shown coupled to an implant. The microanchor device 3 may be coupled directly to an end of a tubular member in an evenly spaced distribution around the outside surface of the tubular member. In FIG. 3C the microanchor device is shown in a retracted state on the outside surface of a tubular member 16 and in FIG. 3D the microanchor device 3 is shown in an engaged state on the outside surface of the tubular member 16. The location of the anchoring devices 3 with respect to the tubular member or implanted device may be coupled together in any pattern.

In FIGS. 4A-4D, another alternative embodiment of the present invention is shown. The microanchor device 4 is similar to the embodiment of FIGS. 2A and 2B. The microanchor device 4 may have two tissue engaging portions 42. Each of the tissue engaging portions 42 may be coupled to a device engagement portion 44 with a connector portion 46 therebetween. The tissue engagement member 42 of the microanchor device 4 may allow the device to couple to a body tissue when implanted into a patient. The size and shape of the tissue engagement member 42 is designed to limit the depth of tissue wall penetration to the submucosa layer of the tissue wall. The limit on tissue penetration depth may allow the microanchor device 4 to be removed from the tissue wall and also limit any damage that may be caused by the tissue engagement member 42.

The connector portions 46 may provide a strain relief when the microanchor device 4 is implanted into a body lumen. As forces from the body act upon a device (See FIGS. 4B-4D) coupled to the microanchor device 4, the connector portions 46 may stretch or deform in order to reduce the force that may be translated to the tissue engaging portions 42. The reduction of force on the tissue engagement portions 42 may prevent the tissue engagement portions from pulling out of the tissue wall and also may prevent an implanted device from migrating or moving from the implanted location. A device might consist of a sleeve device 16 as shown in FIGS. 4B and 4C, or a stent frame 19 in combination with a sleeve device 16 as shown in FIG. 4D. Including multiple microanchor devices 4 on an implantable device may further reduce the likelihood of a device from being removed prematurely from an implant site.

In another embodiment, similar to the embodiment in FIG. 1A, illustrated in FIG. 5, a microanchor device 5 in an open configuration is illustrated having a first tissue engagement member and second tissue engagement member joined by a connector 12. Connector 12 in this embodiment is two coil springs made of a metal such as nitinol or stainless steel. The spacing between the coil springs can be changed to provide greater or lesser distance between the tissue engagement members. Multiple coil springs, such as two or three or more, may be used to provide different anchoring forces and angles to suit the different microanchor requirements of the anatomy.

Other embodiments contemplated include using a combination of the microanchor devices described herein by coupling one or more of microanchor devices 1-5, in any array or pattern, to any implantable device. In some embodiments, this plurality of varying anchoring devices, will extend along the length of the implantable device. The microanchor devices may be coupled to the implantable device in varying directions. The different angular placement of the microanchor devices will allow the individual microanchor devices to absorb forces from multiple directions when implanted into the body.

While particular embodiments of the present invention have been illustrated and described herein, the present invention should not be limited to such illustrations and descriptions. It should be apparent that changes and modifications may be incorporated and embodied as part of the present invention within the scope of the following claims.

Example:

A microanchor similar to that depicted in FIG. 1 was produced by first obtaining 0.018″ diameter nitinol wire (Ft. Wayne Metals, Ft. Wayne, IN). A metal fixture was made having three rods mounted parallel to one another with a small gap therebetween. The nitinol wire was then wound in serpentine fashion around the three rods and secured such that the two ends of the wire wrapped completely around the outer two rods. Heat treatment of the serpentine shaped nitinol wire was accomplished by placing the fixture with the nitinol wire in a fluidized bed furnace at 480° C. for 7 minutes. The fixture having the nitinol wire was removed from the oven and quenched in water. After quenching, the nitinol wire was removed from the fixture. As a result of the thermal treatment, the wire retained its serpentine configuration. The outer loops were then trimmed to produce sharp points at a position approximately 200 degrees around the outer rods respectively.

The serpentine shaped nitinol wire was then preloaded by wrapping it around a single small diameter rod until it generally assumed the shape shown in FIG. 1A. A piece of suture was used to tie a quick-release knot at the crossover portion of the loaded nitinol wire.

Next, the trained and locked nitinol microanchor was evaluated for tissue retention performance. To simulate a stent frame, the locked microanchor was affixed to a small diameter rod. A piece of canine duodenum was used as the representative tissue. The microanchor was held against the tissue and the suture quick-release pulled to release the microanchor. The microanchor immediately unwound so that the two pincer ends of the microanchor anchor themselves into the tissue.

Load bearing performance of the anchored microanchor was determined by tying a string to the loop of the microanchor and vertically hanging a weight on the opposite end of this string. A starting weight of 20 gm was used. The weight was allowed to hang for approximately 5 minutes. If there were no signs of tissue tearing or the microanchor releasing, an additional 20 gm was added. This process was repeated until the weight reached 200 gm. With 200 gm hanging from the microanchor and after about 3 minutes the microanchor released itself from the tissue. There was no tearing of the tissue. 

The invention claimed is:
 1. An implantable device comprising: a body configured to be implanted in a body lumen of a patient; and a microanchor including, a first portion attached to the body, a second portion having at least one tissue engagement member configured to penetrate tissue of a wall of a body lumen by less than or equal to 1 mm and greater than 0 mm, and a reversibly deformable and recoverable segment located between said first portion and the second portion.
 2. The implantable device of claim 1, wherein the m icroanchor is formed of stainless steel.
 3. The implantable device of claim 1, wherein the m icroanchor is formed of nitinol.
 4. The implantable device of claim 1, wherein the reversibly deformable and recoverable segment defines an “S” shape.
 5. The implantable device of claim 1, wherein the first portion of the m icroanchor includes a loop engaged with the body of the implantable device.
 6. The implantable device of claim 1, further comprising a plurality of microanchors attached to the body.
 7. An endoluminal anchoring element comprising: a proximal portion adapted for attachment to an endoluminal device; a distal portion adapted for attachment to a wall of a body lumen; and a reversibly deformable and recoverable segment between said proximal and distal portions providing strain relief between the proximal and distal portions of the anchoring element.
 8. The endoluminal anchoring element of claim 7, wherein the proximal portion comprises a loop adapted to engage with the endoluminal device.
 9. The endoluminal anchoring element of claim 7, wherein the distal portion is configured to penetrate tissue of a wall of a body lumen by about 1 mm.
 10. A microanchor configured to be implanted in a body of a patient, the microanchor com prising: a first portion configured to be attached to an implantable device; a second portion having a tissue engagement member; and a reversibly deformable and recoverable segment located between said first portion and second portion, the reversibly deformable and recoverable segment defining a substantially “S” shape for providing strain relief that absorbs external forces between the device and the wall of the body lumen, and wherein the first portion includes a loop engaged with the device.
 11. A microanchor according to claim 10, wherein at least one of the first portion, the second portion, and the reversibly deformable and recoverable segment is formed of stainless steel.
 12. A microanchor according to claim 10, wherein at least one of the first portion, the second portion, and the reversibly deformable and recoverable segment is formed of nitinol.
 13. A microanchor according to claim 10, wherein the tissue engagement member is adapted to penetrate tissue by 1 mm or less.
 14. An endoluminal anchoring element comprising: a proximal end adapted for attachment to an endolumenal device; a distal end adapted for attachment to a wall of a body lumen; and a reversibly deformable and recoverable segment between said proximal and distal ends, wherein the reversibly deformable and recoverable segment comprises a substantially “S” shape for providing strain relief that absorbs external forces between the endolumenal device and the wall of the body lumen, and wherein the proximal end comprises a loop engaged with the endolumenal device, and the endolumenal anchoring elements are attached in randomly to the endolumenal device.
 15. An implantable medical device system comprising: an implantable device configured to be anchored within a body lumen; a plurality of microanchors for fixating the implantable device within the body lumen, the microanchors being mounted around a portion of the implantable device, each of the microanchors including, a first portion attached to the implantable device; a second portion having a tissue engagement member for insertion into a wall of the body lumen; a reversibly deformable and recoverable segment located between the first portion and the second portion of the microanchor; wherein the reversibly deformable and recoverable segment is substantially “S” shaped and the “S” shaped, reversibly deformable and recoverable segment is configured to stretch or lengthen to absorb a force applied to the first portion.
 16. The system of claim 15, wherein said microanchors are formed of stainless steel.
 17. The system of claim 15, wherein the microanchors are formed of nitinol.
 18. The system of claim 15, wherein the first portion encircles a portion of the implantable deice. 